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第二代H1抗组胺药依巴斯汀、西替利嗪和氯雷他定在临床前模型中的抗组胺作用比较

Comparative antiallergic effects of second-generation H1-antihistamines ebastine, cetirizine and loratadine in preclinical models.

作者信息

Llupià Josep, Gras Jordi, Llenas Jesús

机构信息

Department of Pharmacological Development, Almirall Prodesfarma, Research Centre, Cardener 68-74, 08024-Barcelona, Spain.

出版信息

Arzneimittelforschung. 2003;53(2):93-7. doi: 10.1055/s-0031-1297078.

Abstract

Ebastine (CAS 90729-43-4), cetirizine (CAS 83881-51-0) and loratadine (CAS 79794-75-5) are second generation H1-antihistamines of proven efficacy for treating allergy. Recent clinical studies have found ebastine to be more effective than cetirizine or loratadine in alleviating the symptoms of seasonal allergic rhinitis. The objective of this study was to compare the efficacy of these compounds in three guinea-pig modeles of bronchoconstriction, elicited either by histamine, allergen or leukotriene C4 in order to shed light onto the mechanisms that might explain differences found in clinical studies. In the present experiments, ebastine and cetirizine were equipotent against aerosol histamine-induced bronchospasm in guinea pigs (ED50 115 and 100 micrograms/kg p.o., respectively), while loratadine was three-fold less potent. In the same model the effects of ebastine, loratadine and cetirizine lasted 21, 19 and 15 h, respectively. Ebastine (ED50 334 micrograms/kg p.o.) was the most potent compound in inhibiting allergen-induced bronchospasm in conscious guinea pigs. In vitro studies in tracheally perfused guinea pig lungs demonstrated that ebastine and loratadine inhibited with equal potency the bronchoconstriction induced by leukotriene C4 whilst cetirizine was significantly less potent. Finally, in another in vivo study, ebastine reverted the changes in pulmonary resistance induced by leukotriene C4 in anaesthetised guinea pigs, whereas cetirizine and loratadine were devoid of activity in this model. In accordance with the clinical data, ebastine proved to be the substance with the widest range of application in animal experiments, too.

摘要

依巴斯汀(CAS 90729 - 43 - 4)、西替利嗪(CAS 83881 - 51 - 0)和氯雷他定(CAS 79794 - 75 - 5)是已证实对治疗过敏有效的第二代H1抗组胺药。最近的临床研究发现,依巴斯汀在缓解季节性过敏性鼻炎症状方面比西替利嗪或氯雷他定更有效。本研究的目的是比较这些化合物在三种由组胺、变应原或白三烯C4引发的豚鼠支气管收缩模型中的疗效,以便阐明可能解释临床研究中发现差异的机制。在本实验中,依巴斯汀和西替利嗪对豚鼠气溶胶组胺诱导的支气管痉挛具有同等效力(口服ED50分别为115和100微克/千克),而氯雷他定的效力则低三倍。在同一模型中,依巴斯汀、氯雷他定和西替利嗪的作用分别持续21、19和15小时。依巴斯汀(口服ED50 334微克/千克)是抑制清醒豚鼠变应原诱导的支气管痉挛中效力最强的化合物。在气管灌注豚鼠肺的体外研究表明,依巴斯汀和氯雷他定对白三烯C4诱导的支气管收缩具有同等效力的抑制作用,而西替利嗪的效力明显较低。最后,在另一项体内研究中,依巴斯汀可逆转麻醉豚鼠中白三烯C4诱导的肺阻力变化,而西替利嗪和氯雷他定在该模型中无活性。与临床数据一致,依巴斯汀在动物实验中也被证明是应用范围最广的药物。

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